TY - JOUR
T1 - Mo3S132− Intercalated Layered Double Hydroxide
T2 - Highly Selective Removal of Heavy Metals and Simultaneous Reduction of Ag+ Ions to Metallic Ag0 Ribbons
AU - Yang, Lixiao
AU - Xie, Linxia
AU - Chu, Menglin
AU - Wang, Hui
AU - Yuan, Mengwei
AU - Yu, Zihuan
AU - Wang, Chaonan
AU - Yao, Huiqin
AU - Islam, Saiful M.
AU - Shi, Keren
AU - Yan, Dongpeng
AU - Ma, Shulan
AU - Kanatzidis, Mercouri G.
N1 - Funding Information:
This work is supported by National Natural Science Foundation of China (No. U1832152 and 22176017), Ningxia Key research and Development Program (No. 2018BEG03017), Natural Science Foundation of Ningxia (2020AAC03115), China Postdoctoral Science Foundation (2020M680430), Foundation of State Key Laboratory of High‐efficiency Utilization of Coal and Green Chemical Engineering (No. 2020‐KF‐40). At Northwestern University this work was partially supported by National Science Foundation Grant DMR‐2003476.
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2022/1/3
Y1 - 2022/1/3
N2 - We demonstrate a new material by intercalating Mo3S132− into Mg/Al layered double hydroxide (abbr. Mo3S13-LDH), exhibiting excellent capture capability for toxic Hg2+ and noble metal silver (Ag). The as-prepared Mo3S13-LDH displays ultra-high selectivity of Ag+, Hg2+ and Cu2+ in the presence of various competitive ions, with the order of Ag+>Hg2+>Cu2+>Pb2+≥Co2+, Ni2+, Zn2+, Cd2+. For Ag+ and Hg2+, extremely fast adsorption rates (≈90 % within 10 min, >99 % in 1 h) are observed. Much high selectivity is present for Ag+ and Cu2+, especially for trace amounts of Ag+ (≈1 ppm), achieving a large separation factor (SFAg/Cu) of ≈8000 at the large Cu/Ag ratio of 520. The overwhelming adsorption capacities for Ag+ (qmAg=1073 mg g−1) and Hg2+ (qmHg=594 mg g−1) place the Mo3S13-LDH at the top of performing sorbent materials. Most importantly, Mo3S13-LDH captures Ag+ via two paths: a) formation of Ag2S due to Ag-S complexation and precipitation, and b) reduction of Ag+ to metallic silver (Ag0). The Mo3S13-LDH is a promising material to extract low-grade silver from copper-rich minerals and trap highly toxic Hg2+ from polluted water.
AB - We demonstrate a new material by intercalating Mo3S132− into Mg/Al layered double hydroxide (abbr. Mo3S13-LDH), exhibiting excellent capture capability for toxic Hg2+ and noble metal silver (Ag). The as-prepared Mo3S13-LDH displays ultra-high selectivity of Ag+, Hg2+ and Cu2+ in the presence of various competitive ions, with the order of Ag+>Hg2+>Cu2+>Pb2+≥Co2+, Ni2+, Zn2+, Cd2+. For Ag+ and Hg2+, extremely fast adsorption rates (≈90 % within 10 min, >99 % in 1 h) are observed. Much high selectivity is present for Ag+ and Cu2+, especially for trace amounts of Ag+ (≈1 ppm), achieving a large separation factor (SFAg/Cu) of ≈8000 at the large Cu/Ag ratio of 520. The overwhelming adsorption capacities for Ag+ (qmAg=1073 mg g−1) and Hg2+ (qmHg=594 mg g−1) place the Mo3S13-LDH at the top of performing sorbent materials. Most importantly, Mo3S13-LDH captures Ag+ via two paths: a) formation of Ag2S due to Ag-S complexation and precipitation, and b) reduction of Ag+ to metallic silver (Ag0). The Mo3S13-LDH is a promising material to extract low-grade silver from copper-rich minerals and trap highly toxic Hg2+ from polluted water.
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U2 - 10.1002/anie.202112511
DO - 10.1002/anie.202112511
M3 - Article
C2 - 34709699
AN - SCOPUS:85119657683
SN - 1433-7851
VL - 61
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 1
M1 - e202112511
ER -